ENST00000399503.4:c.1754G>C
MANE Select
|
ENSP00000382423.3:p.Arg585Thr
|
|
ENST00000399503.3:c.1754G>C
|
ENSP00000382423.3:p.Arg585Thr
|
|
NM_005921.1:c.1754G>C
|
NP_005912.1:p.Arg585Thr
|
|
XM_005248519.3:c.1376G>C
|
XP_005248576.2:p.Arg459Thr
|
|
XM_011543406.1:c.1499G>C
|
XP_011541708.1:p.Arg500Thr
|
|
XM_011543407.1:c.1686+2094G>C
|
XP_011541709.1:n.1686+2094G>C
|
|
XM_011543408.1:c.1754G>C
|
XP_011541710.1:p.Arg585Thr
|
|
XM_017009484.1:c.1343G>C
|
XP_016864973.1:p.Arg448Thr
|
|
XM_017009485.1:c.1265G>C
|
XP_016864974.1:p.Arg422Thr
|
|
XR_001742068.2:n.1785G>C
|
|
|
NM_005921.2:c.1754G>C
MANE Select
|
NP_005912.1:p.Arg585Thr
|
|